chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
94634566846345669T-22GENICheterozygous52392299
94634674746346748TC22GENIChomozygous51935677
94635401546354016TTAC14GENICpossibly homozygous52195251
94636333146363332GT48GENICheterozygous51935680
94636786046367864TCTC----21GENICheterozygous52392301
94639577246395773AC20GENIChomozygous51935690
94639598246395983T-10GENICheterozygous52195435
94639598346395984C-5GENICheterozygous52195437
94639696546396967GT--5GENICheterozygous51935697
94640739946407400GT53GENICheterozygous52392304
94641412146414122GT40GENICpossibly homozygous51935698
94641414046414141AT39GENIChomozygous51935701
94641414346414144GGT36GENIChomozygous51935704
94641414746414148AG40GENICpossibly homozygous51935707
94641414846414149GC40GENICpossibly homozygous51935711
94641742646417428CA--10GENIChomozygous51935714
94642879446428795TC29GENICheterozygous52392306
94642882446428825G-4GENICheterozygous51935717
94642888946428890TA38GENICheterozygous52195723
94642934146429342AT121GENICheterozygous51935723
94642987946429880GC148GENICheterozygous51935726
94642996746429968CT96GENICheterozygous51935729
94638979346389794TC38GENIChomozygous52757285
94642923946429240CT63GENICheterozygous52544071
94642924446429245AC67GENICheterozygous52544073